F Giraud, J F Mattei, M G Mattei, S Ayme, R Bernard
{"title":"[三染色体细胞4 p。三个新的观察[作者的翻译]。","authors":"F Giraud, J F Mattei, M G Mattei, S Ayme, R Bernard","doi":"10.1007/BF00291941","DOIUrl":null,"url":null,"abstract":"<p><p>Three new observations of trisomy 4p are reported. Two are due to a maternal translocation t(4;15). The third is due to a \"mirror\" duplication, it is the first case of trisomy 4p without balanced parental rearrangement. The very characteristic phenotype is compared to that of 13 other patients already reported in the literature.</p>","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"30 2","pages":"99-108"},"PeriodicalIF":0.0000,"publicationDate":"1975-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00291941","citationCount":"8","resultStr":"{\"title\":\"[Trisomy 4p. Three new observations (author's transl)].\",\"authors\":\"F Giraud, J F Mattei, M G Mattei, S Ayme, R Bernard\",\"doi\":\"10.1007/BF00291941\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Three new observations of trisomy 4p are reported. Two are due to a maternal translocation t(4;15). The third is due to a \\\"mirror\\\" duplication, it is the first case of trisomy 4p without balanced parental rearrangement. The very characteristic phenotype is compared to that of 13 other patients already reported in the literature.</p>\",\"PeriodicalId\":75916,\"journal\":{\"name\":\"Humangenetik\",\"volume\":\"30 2\",\"pages\":\"99-108\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/BF00291941\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Humangenetik\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/BF00291941\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Humangenetik","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/BF00291941","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Trisomy 4p. Three new observations (author's transl)].
Three new observations of trisomy 4p are reported. Two are due to a maternal translocation t(4;15). The third is due to a "mirror" duplication, it is the first case of trisomy 4p without balanced parental rearrangement. The very characteristic phenotype is compared to that of 13 other patients already reported in the literature.